Highly diastereoselective TiCl < inf > 4 < /inf > mediated addition of (E)-cinnamyl(tributyl)tin to α-keto esters

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Sreenivasulu, Bandaru
dc.date.accessioned 2022-03-27T09:02:55Z
dc.date.available 2022-03-27T09:02:55Z
dc.date.issued 2002-04-15
dc.description.abstract Highly syn-(87-98%) diastereoselective addition of (E)-cinnamyl(tributyl)tin to α-keto esters under the influence of titanium tetrachloride, leading to the isolation of pure alkyl syn-2-aryl-2-hydroxy-3-phenylpent-4-enoates in 50-80% yields, is described. © 2002 Elsevier Science Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.43(16)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/S0040-4039(02)00417-3
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403902004173
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12328
dc.subject α-keto esters
dc.subject Allylation
dc.subject Cinnamyl(tributyl)tin
dc.subject Diastereoselectivity
dc.subject Titanium tetrachloride
dc.title Highly diastereoselective TiCl < inf > 4 < /inf > mediated addition of (E)-cinnamyl(tributyl)tin to α-keto esters
dc.type Journal. Article
dspace.entity.type
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